Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61751507 | 1.000 | 0.080 | 10 | 100069757 | missense variant | C/T | snv | 4.2E-02 | 3.4E-02 | 1 | |
rs558683362 | 1.000 | 0.120 | 4 | 1000895 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs141371306 | 1.000 | 0.080 | 13 | 100111886 | missense variant | C/T | snv | 2.0E-05 | 5.6E-05 | 1 | |
rs374993554 | 0.925 | 7 | 100113899 | missense variant | A/G;T | snv | 3.2E-05 | 1 | |||
rs727503778 | 0.925 | 0.080 | 7 | 100114074 | missense variant | G/A | snv | 1 | |||
rs876661307 | 1.000 | 1 | 100123231 | missense variant | A/G | snv | 1 | ||||
rs367737727 | 1.000 | 0.080 | 14 | 100128600 | missense variant | C/T | snv | 1.1E-05 | 1 | ||
rs992336192 | 1.000 | 0.120 | 4 | 1001506 | missense variant | G/A;C | snv | 1 | |||
rs754154200 | 1.000 | 0.120 | 4 | 1001518 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs202247814 | 1.000 | 0.080 | 13 | 100155090 | missense variant | G/A | snv | 1 | |||
rs1430681871 | 1.000 | 0.120 | 4 | 1001712 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1230234600 | 1.000 | 0.120 | 4 | 1001745 | missense variant | G/A;C | snv | 1 | |||
rs1333017606 | 1.000 | 0.080 | 7 | 100175622 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs148789453 | 0.882 | 0.120 | 4 | 1001802 | missense variant | T/A;G | snv | 2.2E-05; 4.4E-06 | 1 | ||
rs876661322 | 1.000 | 10 | 100183802 | missense variant | C/A | snv | 1 | ||||
rs863225072 | 1.000 | 0.160 | 4 | 10019000 | missense variant | A/C | snv | 6.5E-06 | 2.8E-05 | 1 | |
rs369090960 | 1.000 | 0.120 | 4 | 1001982 | missense variant | G/A;C | snv | 2.1E-05; 5.2E-06 | 1 | ||
rs12021720 | 0.925 | 0.160 | 1 | 100206504 | missense variant | T/A;C | snv | 0.92 | 1 | ||
rs202247815 | 1.000 | 0.080 | 13 | 100209354 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs121964999 | 0.882 | 0.120 | 1 | 100214929 | missense variant | A/C | snv | 1.1E-04 | 1.0E-04 | 1 | |
rs199801029 | 0.925 | 0.120 | 4 | 1002275 | missense variant | G/C | snv | 6.6E-05 | 7.7E-05 | 1 | |
rs121965001 | 1.000 | 0.120 | 1 | 100230872 | missense variant | G/C | snv | 1 | |||
rs121965033 | 0.925 | 0.120 | 4 | 1002333 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
rs746766617 | 0.882 | 0.120 | 4 | 1002340 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
rs368454909 | 1.000 | 0.120 | 4 | 1002341 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |